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Design, Synthesis and Aromaticity of an Alternating Cyclo[4]Thiophene[4]Furan

https://doi.org/10.1002/chem.202300477

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

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Polyfurans: A Computational Study

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Emerging applications of carbon nanohoops

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C–C bond formation through oxidatively induced elimination of platinum complexes—A novel approach towards conjugated macrocyclesElectronic supplementary information (ESI) available: experimental section. See http://www.rsc.org/suppdata/cc/b3/b300542a/

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Molecular and electronic structure of cyclo[10]thiophene in various oxidation states: polaron pair vs. bipolaron

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Design and preparation of new palladium precatalysts for C–C and C–N cross-coupling reactions

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Multifunctional π-expanded oligothiophene macrocycles

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Local and global aromaticity in a molecular carbon nanobelt: insights from magnetic response properties in neutral and charged species

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Symmetry breaking and the turn-on fluorescence of small, highly strained carbon nanohoops

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A macrocyclic oligofuran: synthesis, solid state structure and electronic properties

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A diketopyrrolopyrrole-based macrocyclic conjugated molecule for organic electronics

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Reversible redox switching between local and global aromaticity for core-modified expanded carbaisophlorinoids

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Design, synthesis, and properties of a six-membered oligofuran macrocycle

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Sigma–pi separation of the electron localization function and aromaticity

inferredcites →https://doi.org/10.1063/1.474701openalex-snapshot

Combined ab initio and density functional study on polaron to bipolaron transitions in oligophenyls and oligothiophenes

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A Saddle-shaped Macrocycle Comprising 2,5-Diphenylthiophene Units

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Optical properties of fully conjugated cyclo[n]thiophenes – An experimental and theoretical approach

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Meaning and Functional Form of the Electron Localization Function

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.12688/openreseurope.19690.1zenodo-depositor-declared

Concealed antiaromaticity

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Alkylnitrogen Compounds: Compounds With N-N, N-P, N-As, N-Sb, N-Bi, N-Si, N-Ge, N-B, and N-Metal Functional Groups

inferred← citeshttps://doi.org/10.1016/b978-0-443-33494-8.00022-6openalex-snapshot

Eight-membered and larger rings

inferred← citeshttps://doi.org/10.1016/j.checat.2023.100830openalex-snapshot

Single-site palladium on sulfur-doped carbon for olefin alkoxycarbonylation: Performance determined by coordination environments

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Precise Synthesis of Ester-Functionalized Cyclo[6]- and Cyclo[7]furans

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